Purity in Practice
Committed to Care, Backed by Precision
At Aqua Charge Lifescience, quality is not a department—it’s a discipline woven into every step of our operations. From sourcing raw materials to the final seal of each IV fluid bottle, our team follows rigorous standards to ensure safety, sterility, and consistency. Because we believe every drop matters when it comes to patient care.
Advanced BFS Technology – Built for Unmatched Sterility
Our production facility features cutting-edge Blow-Fill-Seal (BFS) technology, one of the most advanced and reliable methods for manufacturing sterile IV fluids. This fully automated process integrates container formation, filling, and sealing into a single continuous cycle—all within a closed, sterile environment with no human intervention. As a result, every unit produced is uniform, contamination-free, and tamper-evident.
The BFS process is carried out in a Class 100 aseptic zone, offering the highest level of microbial control. Since the plastic container is formed, filled, and sealed in one uninterrupted sequence, the risk of contamination from external exposure is virtually eliminated. This integrated design not only ensures product sterility but also guarantees precision dosing, as each bottle is filled with exceptional accuracy and consistency.
What Defines Our Quality Approach?
At Aqua Charge Lifescience, quality isn’t just a department—it’s the foundation of everything we do. Our approach is rooted in rigorous systems, advanced infrastructure, and an uncompromising commitment to patient safety. From sourcing to shipping, every step is engineered to deliver trust and therapeutic reliability.
End-to-End Quality Control
From raw material testing to final product release, every batch undergoes strict in-process and final quality checks. Our dedicated QA/QC teams ensure that only products meeting the highest safety and efficacy standards are approved for distribution
Regulatory Compliance & GMP Standards
Our facility follows Good Manufacturing Practices (GMP) under Schedule M, with SOP-driven processes, full traceability, and audit readiness. We meet all necessary quality standards for sterile injectable and large-volume parenteral manufacturing.
Sterile Manufacturing Infrastructure
Skilled Workforce & Quality-Centric Culture
Our highly trained professionals follow detailed SOPs and adhere to strict quality protocols at every level. Through regular training, supervision, and cross-functional coordination, we maintain a company-wide commitment to excellence in every unit produced.
What Defines Our Quality Approach?
At Aqua Charge Lifescience, quality isn’t just a department—it’s the foundation of everything we do. Our approach is rooted in rigorous systems, advanced infrastructure, and an uncompromising commitment to patient safety. From sourcing to shipping, every step is engineered to deliver trust and therapeutic reliability.
End-to-End Quality Control
From raw material testing to final product release, every batch undergoes strict in-process and final quality checks. Our dedicated QA/QC teams ensure that only products meeting the highest safety and efficacy standards are approved for distribution
Regulatory Compliance & GMP Standards
Our facility follows Good Manufacturing Practices (GMP) under Schedule M, with SOP-driven processes, full traceability, and audit readiness. We meet all necessary quality standards for sterile injectable and large-volume parenteral manufacturing.
Sterile Manufacturing Infrastructure
Skilled Workforce & Quality-Centric Culture
Our highly trained professionals follow detailed SOPs and adhere to strict quality protocols at every level. Through regular training, supervision, and cross-functional coordination, we maintain a company-wide commitment to excellence in every unit produced.
Documentation & Traceability
Our documentation system ensures full traceability and regulatory compliance. Detailed Batch Manufacturing and Packaging Records (BMRs & BPRs) are maintained and reviewed by QA. Real-time digital and physical logs enable tracking from raw materials to finished goods. Each step is time-stamped, auditable, and securely archived—simplifying audits and enabling efficient recall procedures when needed.
Continuous Quality Improvement (CQI)
We follow a proactive approach to quality through continuous improvement. Internal audits, CAPA systems, and change control processes help us maintain high standards. Supplier performance is regularly reviewed, and all staff undergo routine training updates. Feedback from healthcare professionals and partners is systematically evaluated and used to strengthen our systems.
In-Process & Final Product Testing
At Aqua Charge Lifescience, quality is built into every stage of manufacturing—not just checked at the end. We perform rigorous in-process controls (IPQC) such as real-time pH, temperature, conductivity, and osmolality checks, as well as visual and volume inspections during production. Final products undergo comprehensive testing in our QC lab, including sterility, endotoxin, particulate matter, pH, and vacuum integrity checks. Only batches meeting all critical quality attributes are approved, with retention samples archived for reference.
